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Temporal evolution of single-cell transcriptomes of Drosophila olfactory projection neurons

Neurons undergo substantial morphological and functional changes during development to form precise synaptic connections and acquire specific physiological properties. What are the underlying transcriptomic bases? Here, we obtained the single-cell transcriptomes of Drosophila olfactory projection ne...

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Autores principales: Xie, Qijing, Brbic, Maria, Horns, Felix, Kolluru, Sai Saroja, Jones, Robert C, Li, Jiefu, Reddy, Anay R, Xie, Anthony, Kohani, Sayeh, Li, Zhuoran, McLaughlin, Colleen N, Li, Tongchao, Xu, Chuanyun, Vacek, David, Luginbuhl, David J, Leskovec, Jure, Quake, Stephen R, Luo, Liqun, Li, Hongjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870145/
https://www.ncbi.nlm.nih.gov/pubmed/33427646
http://dx.doi.org/10.7554/eLife.63450
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author Xie, Qijing
Brbic, Maria
Horns, Felix
Kolluru, Sai Saroja
Jones, Robert C
Li, Jiefu
Reddy, Anay R
Xie, Anthony
Kohani, Sayeh
Li, Zhuoran
McLaughlin, Colleen N
Li, Tongchao
Xu, Chuanyun
Vacek, David
Luginbuhl, David J
Leskovec, Jure
Quake, Stephen R
Luo, Liqun
Li, Hongjie
author_facet Xie, Qijing
Brbic, Maria
Horns, Felix
Kolluru, Sai Saroja
Jones, Robert C
Li, Jiefu
Reddy, Anay R
Xie, Anthony
Kohani, Sayeh
Li, Zhuoran
McLaughlin, Colleen N
Li, Tongchao
Xu, Chuanyun
Vacek, David
Luginbuhl, David J
Leskovec, Jure
Quake, Stephen R
Luo, Liqun
Li, Hongjie
author_sort Xie, Qijing
collection PubMed
description Neurons undergo substantial morphological and functional changes during development to form precise synaptic connections and acquire specific physiological properties. What are the underlying transcriptomic bases? Here, we obtained the single-cell transcriptomes of Drosophila olfactory projection neurons (PNs) at four developmental stages. We decoded the identity of 21 transcriptomic clusters corresponding to 20 PN types and developed methods to match transcriptomic clusters representing the same PN type across development. We discovered that PN transcriptomes reflect unique biological processes unfolding at each stage—neurite growth and pruning during metamorphosis at an early pupal stage; peaked transcriptomic diversity during olfactory circuit assembly at mid-pupal stages; and neuronal signaling in adults. At early developmental stages, PN types with adjacent birth order share similar transcriptomes. Together, our work reveals principles of cellular diversity during brain development and provides a resource for future studies of neural development in PNs and other neuronal types.
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spelling pubmed-78701452021-02-10 Temporal evolution of single-cell transcriptomes of Drosophila olfactory projection neurons Xie, Qijing Brbic, Maria Horns, Felix Kolluru, Sai Saroja Jones, Robert C Li, Jiefu Reddy, Anay R Xie, Anthony Kohani, Sayeh Li, Zhuoran McLaughlin, Colleen N Li, Tongchao Xu, Chuanyun Vacek, David Luginbuhl, David J Leskovec, Jure Quake, Stephen R Luo, Liqun Li, Hongjie eLife Neuroscience Neurons undergo substantial morphological and functional changes during development to form precise synaptic connections and acquire specific physiological properties. What are the underlying transcriptomic bases? Here, we obtained the single-cell transcriptomes of Drosophila olfactory projection neurons (PNs) at four developmental stages. We decoded the identity of 21 transcriptomic clusters corresponding to 20 PN types and developed methods to match transcriptomic clusters representing the same PN type across development. We discovered that PN transcriptomes reflect unique biological processes unfolding at each stage—neurite growth and pruning during metamorphosis at an early pupal stage; peaked transcriptomic diversity during olfactory circuit assembly at mid-pupal stages; and neuronal signaling in adults. At early developmental stages, PN types with adjacent birth order share similar transcriptomes. Together, our work reveals principles of cellular diversity during brain development and provides a resource for future studies of neural development in PNs and other neuronal types. eLife Sciences Publications, Ltd 2021-01-11 /pmc/articles/PMC7870145/ /pubmed/33427646 http://dx.doi.org/10.7554/eLife.63450 Text en © 2021, Xie et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Xie, Qijing
Brbic, Maria
Horns, Felix
Kolluru, Sai Saroja
Jones, Robert C
Li, Jiefu
Reddy, Anay R
Xie, Anthony
Kohani, Sayeh
Li, Zhuoran
McLaughlin, Colleen N
Li, Tongchao
Xu, Chuanyun
Vacek, David
Luginbuhl, David J
Leskovec, Jure
Quake, Stephen R
Luo, Liqun
Li, Hongjie
Temporal evolution of single-cell transcriptomes of Drosophila olfactory projection neurons
title Temporal evolution of single-cell transcriptomes of Drosophila olfactory projection neurons
title_full Temporal evolution of single-cell transcriptomes of Drosophila olfactory projection neurons
title_fullStr Temporal evolution of single-cell transcriptomes of Drosophila olfactory projection neurons
title_full_unstemmed Temporal evolution of single-cell transcriptomes of Drosophila olfactory projection neurons
title_short Temporal evolution of single-cell transcriptomes of Drosophila olfactory projection neurons
title_sort temporal evolution of single-cell transcriptomes of drosophila olfactory projection neurons
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870145/
https://www.ncbi.nlm.nih.gov/pubmed/33427646
http://dx.doi.org/10.7554/eLife.63450
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